Quantifying the genetic correlation between cancers can provide important insights into the mechanisms driving cancer etiology. Using genome-wide association study summary statistics across six cancer types based on a total of 296,215 cases and 301,319 controls of European ancestry, here we estimate the pair-wise genetic correlations between breast, colorectal, head/neck, lung, ovary and prostate cancer, and between cancers and 38 other diseases. We observed statistically significant genetic correlations between lung and head/neck cancer (rg = 0.57, p = 4.6 × 10-8), breast and ovarian cancer (rg = 0.24, p = 7 × 10-5), breast and lung cancer (rg = 0.18, p =1.5 × 10-6) and breast and colorectal cancer (rg = 0.15, p = 1.1 × 10-4). We also foun...
Previous studies have suggested that polymorphisms in CASP8 on chromosome 2 are associated with brea...
Introduction Late-onset Alzheimer’s disease (LOAD, onset age > 60 years) is the most prevalent demen...
Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathw...
Additional file 1: List of ethical committees that approved the access to the data analyzed in this...
Left-right asymmetry is an important organizing feature of the healthy brain that may be altered in ...
Publisher's version (útgefin grein).Quantifying the genetic correlation between cancers can provide ...
HapMap imputed genome-wide association studies (GWAS) have revealed >50 loci at which common variant...
AG has received support by NordForsk Nordic Trial Alliance (NTA) grant, by Academy of Finland Fello...
Genome-wide studies of patients carrying pathogenic variants (mutations) in BRCA1 or BRCA2 have repo...
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic vari...
In 2020, 146,063 deaths due to pancreatic cancer are estimated to occur in Europe and the United Sta...
PURPOSE: Cis-acting regulatory SNPs resulting in differential allelic expression (DAE) may, in part,...
Publisher's version (útgefin grein)Previous transcriptome-wide association studies (TWAS) have ident...
NBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs...
Genome-wide association studies have found SNPs at 17q22 to be associated with breast cancer risk. T...
Previous studies have suggested that polymorphisms in CASP8 on chromosome 2 are associated with brea...
Introduction Late-onset Alzheimer’s disease (LOAD, onset age > 60 years) is the most prevalent demen...
Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathw...
Additional file 1: List of ethical committees that approved the access to the data analyzed in this...
Left-right asymmetry is an important organizing feature of the healthy brain that may be altered in ...
Publisher's version (útgefin grein).Quantifying the genetic correlation between cancers can provide ...
HapMap imputed genome-wide association studies (GWAS) have revealed >50 loci at which common variant...
AG has received support by NordForsk Nordic Trial Alliance (NTA) grant, by Academy of Finland Fello...
Genome-wide studies of patients carrying pathogenic variants (mutations) in BRCA1 or BRCA2 have repo...
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic vari...
In 2020, 146,063 deaths due to pancreatic cancer are estimated to occur in Europe and the United Sta...
PURPOSE: Cis-acting regulatory SNPs resulting in differential allelic expression (DAE) may, in part,...
Publisher's version (útgefin grein)Previous transcriptome-wide association studies (TWAS) have ident...
NBS1, also known as NBN, plays an important role in maintaining genomic stability. Interestingly, rs...
Genome-wide association studies have found SNPs at 17q22 to be associated with breast cancer risk. T...
Previous studies have suggested that polymorphisms in CASP8 on chromosome 2 are associated with brea...
Introduction Late-onset Alzheimer’s disease (LOAD, onset age > 60 years) is the most prevalent demen...
Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathw...